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Oxaliplatin Added to Fluoropyrimidine/Bevacizumab as Initial Therapy for Unresectable Metastatic Colorectal Cancer in Older Patients: A Multicenter, Randomized, Open-Label Phase III Trial (JCOG1018).
Takashima, Atsuo; Hamaguchi, Tetsuya; Mizusawa, Junki; Nagashima, Fumio; Ando, Masahiko; Ojima, Hitoshi; Denda, Tadamichi; Watanabe, Jun; Shinozaki, Katsunori; Baba, Hideo; Asayama, Masako; Hasegawa, Seiji; Masuishi, Toshiki; Nakata, Ken; Tsukamoto, Shunsuke; Katayama, Hiroshi; Nakamura, Kenichi; Fukuda, Haruhiko; Kanemitsu, Yukihide; Shimada, Yasuhiro.
Afiliação
  • Takashima A; Department of Gastrointestinal Oncology, National Cancer Center Hospital, Tokyo, Japan.
  • Hamaguchi T; Department of Medical Oncology, Saitama Medical University International Medical Center, Saitama, Japan.
  • Mizusawa J; JCOG Data Center/Operations Office, National Cancer Center Hospital, Tokyo, Japan.
  • Nagashima F; Department of Medical Oncology, Kyorin University Faculty of Medicine, Tokyo, Japan.
  • Ando M; Department of Advanced Medicine, Nagoya University Hospital, Nagoya, Japan.
  • Ojima H; Department of Gastroenterological Surgery, Gunma Prefectural Cancer Center, Gunma, Japan.
  • Denda T; Division of Gastroenterology, Chiba Cancer Center, Chiba, Japan.
  • Watanabe J; Department of Surgery, Gastroenterological Center, Yokohama City University Medical Center, Yokohama, Japan.
  • Shinozaki K; Division of Clinical Oncology, Hiroshima Prefectural Hospital, Hiroshima, Japan.
  • Baba H; Department of Gastroenterology, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.
  • Asayama M; Department of Gastroenterology, Saitama Cancer Center, Saitama, Japan.
  • Hasegawa S; Department of Clinical Oncology, Saiseikai Yokohama Nanbu Hospital, Yokohama, Japan.
  • Masuishi T; Department of Clinical Oncology, Aichi Cancer Center Hospital, Nagoya, Japan.
  • Nakata K; Department of Colorectal Surgery, Sakai City Medical Center, Osaka, Japan.
  • Tsukamoto S; Department of Colorectal Surgery, National Cancer Center Hospital, Tokyo, Japan.
  • Katayama H; JCOG Data Center/Operations Office, National Cancer Center Hospital, Tokyo, Japan.
  • Nakamura K; JCOG Data Center/Operations Office, National Cancer Center Hospital, Tokyo, Japan.
  • Fukuda H; JCOG Data Center/Operations Office, National Cancer Center Hospital, Tokyo, Japan.
  • Kanemitsu Y; Department of Colorectal Surgery, National Cancer Center Hospital, Tokyo, Japan.
  • Shimada Y; Department of Clinical Oncology, Kochi Health Sciences Center, Kochi, Japan.
J Clin Oncol ; : JCO2302722, 2024 Aug 26.
Article em En | MEDLINE | ID: mdl-39186709
ABSTRACT

PURPOSE:

Doublet chemotherapy with fluoropyrimidine (FP) and oxaliplatin (OX) plus bevacizumab (BEV) is a standard regimen for unresectable metastatic colorectal cancer (MCRC). However, the efficacy of adding OX to FP plus BEV (FP + BEV) remains unclear for older patients, a population for whom FP + BEV is standard. We aimed to confirm the superiority of adding OX to FP + BEV for this population.

METHODS:

This open-label, randomized, phase III trial was conducted at 42 institutions in Japan. Patients with unresectable MCRC age 70-74 years with Eastern Cooperative Oncology Group performance status (ECOG-PS) 2 and those 75 years and older with ECOG-PS 0-2 were randomly assigned (11) to an FP + BEV arm or an OX addition (FP + BEV + OX) arm. Fluorouracil plus levofolinate calcium or capecitabine was declared before enrollment. The primary end point was progression-free survival (PFS). The study was registered in the Japan Registry of Clinical Trials (identifier jRCTs031180145).

RESULTS:

Between September 2012 and March 2019, 251 patients were randomly assigned to the FP + BEV arm (n = 125) and the FP + BEV + OX arm (n = 126). The median age was 80 and 79 years in the respective arm. The median PFS was 9.4 months (95% CI, 8.3 to 10.3) in the FP + BEV arm and 10.0 months (9.0 to 11.2) in the FP + BEV + OX arm (hazard ratio [HR], 0.84 [90.5% CI, 0.67 to 1.04]; one-sided P = .086). The median overall survival was 21.3 months (18.7 to 24.3) in the FP + BEV arm and 19.7 months (15.5 to 25.5) in the FP + BEV + OX arm (HR, 1.05 [0.81 to 1.37]). The proportion of any grade ≥3 adverse events was higher in the FP + BEV + OX arm (52% v 69%). There was one treatment-related death in the FP + BEV arm and three in the FP + BEV + OX arm.

CONCLUSION:

No benefit of adding OX to FP + BEV as first-line treatment was demonstrated in older patients with MCRC. FP + BEV is recommended for this population.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Clin Oncol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Japão País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Clin Oncol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Japão País de publicação: Estados Unidos